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1 distribution of the cases generated by each infected individual.
2 al becoming infected on contact with another infected individual.
3 sk from contact with oral secretions from an infected individual.
4 -restricted cellular immune responses in HIV-infected individuals.
5 ons (TAMs)) are rare in the virus from HIV-2-infected individuals.
6 that are susceptible to bNAbs isolated from infected individuals.
7 of infectious virus from reservoirs in HIV-1-infected individuals.
8 at Cx43 is dysregulated in the hearts of HIV-infected individuals.
9 uding among antiretroviral therapy-naive HIV-infected individuals.
10 shown to be present in sera from most HIV-1-infected individuals.
11 -infected individuals compared to HIV-1 mono-infected individuals.
12 voir will be necessary to eradicate HIV-1 in infected individuals.
13 ivalent to those in age-matched, chronically infected individuals.
14 M. tuberculosis-specific CD4 T cells in HIV-infected individuals.
15 fective cART, HIV-1 persists indefinitely in infected individuals.
16 eurological damage in virally suppressed HIV-infected individuals.
17 lowing clearance of peripheral virus in ZIKV-infected individuals.
18 d to broadly neutralizing antibodies in some infected individuals.
19 Env-specific antibodies in a minority of HIV-infected individuals.
20 syndrome (HUS), and adverse outcomes in STEC-infected individuals.
21 ar outnumber lymphocytes in the semen of HIV-infected individuals.
22 ted in an independent cohort of latently Mtb-infected individuals.
23 leading to increased fracture rate among HIV-infected individuals.
24 easing opportunities for timely treatment of infected individuals.
25 resent the most common type of cancer in HIV-infected individuals.
26 pment of a greater number of symptoms in WNV-infected individuals.
27 tion (FMT) as a potential therapeutic in HIV-infected individuals.
28 lec-1 in fuelling HIV-1 dissemination within infected individuals.
29 lasma sCD163 levels were measured in 933 HIV-infected individuals.
30 rvoir represents a barrier to cure among HIV-infected individuals.
31 alence estimates to published numbers of HIV-infected individuals.
32 portant determinant of media thinning in HIV-infected individuals.
33 of care in the clinical management of HIV-1-infected individuals.
34 s are available, they are ineffective in HPV-infected individuals.
35 to control HCV infection in the majority of infected individuals.
36 animal models and suppress viremia in HIV-1-infected individuals.
37 te of disease progression will vary in HIV-1 infected individuals.
38 on to evade immunity and reinfect previously infected individuals.
39 sonic activity is significantly lower in HIV-infected individuals.
40 n varies markedly in hepatitis C virus (HCV)-infected individuals.
41 hed and, importantly, how these vary between infected individuals.
42 unotherapeutic approaches in ART-treated HIV-infected individuals.
43 tified 2 human T-lymphotropic virus (HTLV)-4-infected individuals.
44 years), aviremic (<50 HIV RNA copies/ml) HIV-infected individuals.
45 thogen that causes mild to severe colitis in infected individuals.
46 oint host/pathogen genetic data from 541 HIV infected individuals.
47 dults and human immunodeficiency virus (HIV)-infected individuals.
48 ent among human immunodeficiency virus (HIV)-infected individuals.
49 dysfunctions at inflammatory tissue sites in infected individuals.
50 d this might be clinically beneficial to HIV-infected individuals.
51 high rates of cardiovascular disease in HIV-infected individuals.
52 thrombotic therapies should be tested in HIV-infected individuals.
53 Neurogenesis is impaired in HIV-infected individuals.
54 icative advantage and persist in chronically infected individuals.
55 directed bNAbs have been isolated from HIV-1-infected individuals.
56 thogen in human immunodeficiency virus (HIV)-infected individuals.
57 ion was detected in 28 out of 31 chronically infected individuals.
58 ion in macrophages, a key target of HIV-1 in infected individuals.
59 effusion lymphoma) primarily observed in HIV-infected individuals.
60 d be to expand the donor pool to include HIV-infected individuals.
61 diseases requires the accurate detection of infected individuals.
62 ng) stage sexual gametocytes in the blood of infected individuals.
63 idence in human immunodeficiency virus (HIV)-infected individuals.
64 mpairment continues to afflict almost 50% of infected individuals.
65 HIV-1 Gag p24 production in samples from HIV-infected individuals.
66 e sera will be relative to that of sera from infected individuals.
67 inical outcome and is highly variable across infected individuals.
68 to 30% of human immunodeficiency virus (HIV)-infected individuals.
69 between different groups of susceptible and infected individuals.
70 a problem affecting approximately 50% of HIV-infected individuals.
71 G for the treatment of early syphilis in HIV-infected individuals.
72 be large benefits to vaccinating previously infected individuals.
73 ciated with chronic immune activation in HIV-infected individuals.
74 gnitive dysfunction seen in well-treated HIV-infected individuals.
75 infection (HCV) commonly co-occur among HIV-infected individuals.
76 ibodies, whether engineered or isolated from infected individuals.
77 s one of the most common malignancies in HIV-infected individuals.
78 of new drugs aimed at eliminating HIV-1 from infected individuals.
80 significantly higher (P < 0.0001) among HCV-infected individuals (3.31% [24 of 726 samples]) than am
81 ly prolonged the time to AIDS onset in HIV-1-infected individuals, a functional cure has yet to be fo
83 ges (but not T cells) of drug-suppressed HIV-infected individuals also contained abundant uracils.
84 tes to loss of immune control of LTBI in HIV-infected individuals, although the precise mechanisms wh
85 17, and Th22/Tc22 cells in 15 S. stercoralis-infected individuals and 10 uninfected individuals stimu
86 ogenesis have been noted in the brain of HIV-infected individuals and are likely linked to HIV-associ
87 Lymph node inflammation was higher in HIV-infected individuals and correlated with markers of vira
88 antibody response in a cohort of chronically infected individuals and found that a broadly neutralizi
89 ency, are elicited only in a small subset of infected individuals and have yet to be induced by vacci
90 cently identified in hepatitis C virus (HCV)-infected individuals and individuals who had received mu
91 ith an estimated 130-170 million chronically infected individuals and is the cause of serious liver d
92 ibodies elicited by the authentic virus from infected individuals and polyclonal antibodies from vacc
93 bs), and gp41 derived from chronically HIV-1-infected individuals and produced by hybridoma cells.
95 ically in human immunodeficiency virus (HIV)-infected individuals and simian immunodeficiency virus (
96 urocognitive disorders afflict 30-50% of HIV-infected individuals and synaptodendritic injury remains
97 l inflammation was modestly increased in HIV-infected individuals and was positively correlated with
98 including human immunodeficiency virus (HIV)-infected individuals, and pulmonary colonization with P.
99 ss to affordable diagnostics to identify HBV-infected individuals, and to enable linkage to care and
103 ys capable of detecting antibodies in HPgV-2-infected individuals are needed to establish global sero
104 that a small proportion (<20%) of influenza infected individuals are responsible for the production
106 ) T cell clone isolated from an Mtb latently infected individual as a peptide from the Mtb protein, M
107 omparing IDU+/ HCV+ and IDU-/HCV- in 386 HIV-infected individuals as a discovery sample and in 412 in
108 d significantly higher HEV Ag in chronically infected individuals as compared to acutely infected pat
109 e of a differential effect of smoking in HIV-infected individuals as compared to uninfected individua
110 eral hundred sequences were obtained from an infected individual at seven time points over 2 years.
112 els could potentially be used to rank US HIV-infected individuals at higher or lower risk for CVD, th
114 cells were measured longitudinally in 19 HIV-infected individuals before (median, 2 mo) and after ART
115 pletely dominates the microbiota not only in infected individuals but also in most individuals classi
116 munity is protective in the vast majority of infected individuals but can become detrimental if not f
117 py (ART) suppresses viral replication in HIV-infected individuals but does not eliminate the reservoi
118 ently, the rate of BMD decline slowed in HIV-infected individuals but remained greater than the rate
120 heat pulses enhanced thermal tolerance among infected individuals, but the magnitude of the parasitis
121 rP(Sc)) that self-propagates in the brain of infected individuals by converting the normal prion prot
122 tion of the kinetics of HIV-1 suppression in infected individuals by passively administered 3BNC117,
124 1 gene sequences sampled longitudinally from infected individuals can reveal the evolutionary dynamic
125 ng longitudinal Env sequences from a clade C-infected individual (CAP256), we measured the impact of
126 R-122 and miR-200a are greater in HIV/HCV co-infected individuals compared to HIV-1 mono-infected ind
127 -analysis to estimate the odds of HCV in HIV-infected individuals compared with their HIV-negative co
128 fic CD4 T cells was markedly impaired in HIV-infected individuals, compared with HIV-uninfected indiv
129 served that plasma TNF-alpha levels in HIV-1-infected individuals correlated directly with VL levels
130 dendritic cells, from Plasmodium falciparum-infected individuals, correlated with lower parasitemia.
131 Within sorted lymph node cells from four HIV-infected individuals, CXCR5(+) subsets harbored 11-66-fo
132 HSPCs), which allows the virus to persist in infected individuals despite antiretroviral therapy.
133 ratio in human immunodeficiency virus (HIV)-infected individuals despite effective antiretroviral th
134 structural abnormalities were evident in HIV-infected individuals despite fully suppressive antiretro
135 ction with these viruses, only a minority of infected individuals develop a subsequent malignant tumo
139 nging, but understanding how a subset of HIV-infected individuals develops bNAbs may guide immunizati
140 diagnostics for ZIKV are vital because ZIKV-infected individuals display no symptoms or nonspecific
142 nfection in which selection pressures within infected individuals drive rapid intrahost virus microev
143 s between human immunodeficiency virus (HIV)-infected individuals during the first approximately 7.5
144 ring pregnancy could attenuate disease among infected individuals, especially in the context of antib
147 M. tuberculosis-specific CD4 T cells in HIV-infected individuals expressed significantly higher leve
148 1 antiretroviral therapy in prolonging life, infected individuals face lifelong therapy because of a
149 l tracked human immunodeficiency virus (HIV)-infected individuals for 10 years following ART initiati
150 ould be included in routine screening of HIV-infected individuals for sexually transmitted infections
151 ral-naive human immunodeficiency virus (HIV)-infected individuals from 26 countries who were newly di
152 or novel specificities from HIV-1 subtype C infected individuals from India that can be exploited as
153 s collected from 70 virally suppressed HIV-1-infected individuals from Rakai District, Uganda, who ha
154 i individuals, in contrast to uninfected and infected individuals from the sympatric ethnic group Mos
160 s to those with a mild fever and blisters on infected individuals' hands, feet, and throats to infect
161 nctional analysis of T-cell responses in HIV-infected individuals has indicated that virus-specific C
163 ors that are increased in the serum of HIV-1-infected individuals have been suggested to directly or
165 ating persistent viral reservoirs from HIV-1-infected individuals have focused on CD4(+) T-cell reser
166 at central memory CD4 T cells (TCM) from HIV-infected individuals have heightened expression of BCL-2
167 llows for transplantation of organs from HIV-infected individuals (HIV+), provided it is performed un
168 -1-infected cells to ADCC by sera from HIV-1-infected individuals.IMPORTANCE HIV-1 evolved sophistica
169 n of infectious virus from reservoirs in HIV-infected individuals.IMPORTANCE The persistence of HIV r
172 he World Health Organization (WHO) for HIV-1-infected individuals in settings with high infectious di
174 ime PCR, using sera from a cohort of acutely infected individuals, in addition to a cohort of chronic
175 fectiveness and treatment outcomes for HIV-1-infected individuals, including children, worldwide.
178 that can target the viral reservoir in HIV-1-infected individuals is a major goal of HIV-1 research.
180 ratio in human immunodeficiency virus (HIV)-infected individuals is associated with inflammation and
182 exhausted T cells isolated from chronically infected individuals, little is known about when this st
184 ing and treatment of M. genitalium among HIV-infected individuals may be warranted to further underst
186 ted from extracellular vesicles in sera from infected individuals may provide a new tool for diagnosi
187 companying microbiota in Helicobacter pylori-infected individuals might affect disease progression an
189 at could compromise the health status of HIV-infected individuals might not be ethically warranted.
190 falciparum Ag-specific B cell subsets in HIV-infected individuals mirror those in the overall B cell
192 ) T cells in HIV-uninfected (n = 20) and HIV-infected individuals (n = 20) with latent TB infection.
195 individuals, or nonreactive results in HIV-1-infected individuals not on therapy, were observed and u
197 rrence in a well-characterized cohort of HIV-infected individuals on antiretroviral therapy (ART) wit
198 f LRAs (panobinostat or vorinostat) to HIV-1-infected individuals on antiretroviral therapy induces a
199 y in which 15 virologically suppressed HIV-1-infected individuals on antiretroviral therapy received
202 These data show that TB recurrence, in HIV-infected individuals on ART is predicted by biomarkers o
205 icrobiomes of HIV-uninfected (HIV SN) to HIV-infected individuals on long-term ART (HIV+ LTART) from
206 that GS-9620 may be useful for treating HIV-infected individuals on suppressive antiretroviral thera
207 ral blood mononuclear cells (PBMCs) from HIV-infected individuals on suppressive antiretroviral thera
208 ote clearance of the macrophage reservoir in infected individuals on suppressive antiviral therapy.
209 dress the fecal bacterial communities in HIV-infected individuals on two ARV regimens from Mexico.
211 nt phagocytosis assays use IE collected from infected individuals or from in vitro cultures of P. fal
212 o primary data, samples of HCV or HIV-HCV co-infected individuals, or samples relying on self-reporte
215 ariation in the number of cases generated by infected individuals, particularly found in spatially lo
216 ion of the serological status of potentially infected individuals, particularly pregnant women, can b
217 ment era, human immunodeficiency virus (HIV)-infected individuals, particularly those who initiated a
218 nclude targeted monitoring for SCC among HIV-infected individuals, particularly those with low CD4 co
219 of E. histolytica is the cyst, with a single infected individual passing up to 45 million cysts per d
220 rovided significant benefit for asymptomatic infected individuals (pooled incidence rate ratio, 0.62;
224 miR-200a are elevated in ART-treated, HIV-1-infected individuals prior to the development of fatal l
225 mechanism by which some dengue virus (DENV)-infected individuals progress to severe disease is poorl
227 alysis of human immunodeficiency virus (HIV)-infected individuals receiving antiretroviral therapy (A
228 evated in human immunodeficiency virus (HIV)-infected individuals receiving antiretroviral therapy (A
230 (HBV) has been reported in hepatitis C virus-infected individuals receiving direct-acting antiviral (
231 sponses in a longitudinal cohort of 15 HIV-1-infected individuals receiving systemic chemotherapy or
232 can occur in rare instances, the majority of infected individuals remain asymptomatic or present with
234 ution with antiretroviral therapy (ART), HIV-infected individuals remain highly susceptible to tuberc
235 on of atypical MBC phenotypes found in HIV-1-infected individuals results from the loss of naive and
237 nalysis and direct genotyping of 4,233 HIV-1-infected individuals reveals two Glu88Ter homozygous and
240 pective cohort study of 45 chronically HIV-1-infected individuals sharing a similar demographics and
241 Although most herpes simplex virus 1 (HSV-1)-infected individuals shed the virus in their body fluids
242 c17, Th22/Tc22, and Tr1 cells in 26 filariae-infected individuals stimulated with filarial antigen fo
243 terferon for treatment of acute HCV in HIV-1 infected individuals (SWIFT-C) is an open-label, 2-cohor
245 e differences, we propose mapping the routes infected individuals take through "disease space." We fi
247 a consistently higher HCV prevalence in HIV-infected individuals than HIV-negative individuals acros
248 may impact future therapy options for newly infected individuals, the clinical significance of the d
249 d the severity of neurological damage in HIV-infected individuals, the likelihood of cognitive impair
250 life and increased the life span of many HIV-infected individuals, this therapeutic strategy has seve
252 need to specifically consider type among HIV-infected individuals to further understand MI outcomes a
253 y interrogating antibodies isolated from HIV-infected individuals to guide strategies aimed at develo
254 ockdown in resting CD4(+) T cells from HIV-1-infected individuals treated with antiretroviral therapy
257 ORTANCE The persistence of HIV reservoirs in infected individuals under effective antiretroviral trea
258 ndard of care for clinical monitoring of HIV-infected individuals undergoing antiretroviral therapy.
260 and potency of NAb responses in 98 CRF07_BC-infected individuals using a large, multi-subtype panel
261 onal study), clinical scenario (asymptomatic infected individuals vs individuals after endoscopic res
263 Using convalescent plasma from DENV- and WNV-infected individuals, we found substantial enhancement o
264 etramer to detect AMA1-specific B cells, HIV-infected individuals were also shown to have a higher pr
265 from four fully ART-suppressed, chronically infected individuals were assayed at two time points sep
267 Compared with HIV-uninfected persons, HIV-infected individuals were slightly younger (mean age, 52
268 nts (LRA) in resting CD4(+) T cells from HIV-infected individuals were tested, the ultrasensitive p24
269 Approximately half of all MIs among HIV-infected individuals were type 2 MIs caused by heterogen
270 scription factor profiles were skewed in HIV-infected individuals where the proportion of T-bet(high)
271 disorders remain prevalent among HIV type 1-infected individuals, whereas our understanding of the c
273 ation of the gut is rarely achieved in HIV-1-infected individuals who are receiving clinically effect
275 sequential lineages of trimers derived from infected individuals who developed bNAbs, and presenting
276 ca where Chagas disease is endemic and among infected individuals who have migrated to nonendemic are
277 ing referral; and overall proportions of HIV-infected individuals who knew their status (first 90 tar
281 matory predictors of bNAb development in HIV-infected individuals who spontaneously control HIV in th
282 and telomere length were assessed in 94 HIV-infected individuals who were aged >45 years and receivi
283 of unaware and viremic HIV-infected and HCV-infected individuals who were currently not being reache
284 can be dramatically reduced by treating the infected individual with antiretroviral therapy (ART).
285 These observations suggest that recently infected individuals with a delayed NAb response against
286 re recognized at 10-fold-lower levels in Mtb-infected individuals with a history of TB disease less t
287 In analysis that controlled for age, HIV-infected individuals with an undetectable viral load had
288 transcriptomes of monocytes derived from HIV-infected individuals with and without CI using genome-wi
289 n-label dose-finding study, we recruited HIV-infected individuals with cryptococcal meningitis who pr
291 s recently been detected in the brain of HIV-infected individuals with HIV replication in the periphe
292 rgeting strategies in the treatment of virus-infected individuals with impaired IFITM3 activity.
295 CD4 T cell immunity that are impaired in HIV-infected individuals with LTBI, which may contribute to
300 r magnetic resonance at 1.5-T in treated HIV-infected individuals without known cardiovascular diseas
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